A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18256332



Internal ID20823372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:180748000..181393832hg38UCSC Ensembl
chr2:181612727..182258559hg19UCSC Ensembl
Cytoband2q31.3
Allele length
AssemblyAllele length
hg38645833
hg19645833
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6550475
Supporting Variants
Samples
Known GenesMIR4437, SCHLAP1, UBE2E3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18256332
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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